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P Kenna

Showing results (11-20 of 80) with videos related to

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Science (New York, N.Y.)|May 8, 1992
On the molecular genetics of retinitis pigmentosaP Humphries, P Kenna, G J Farrar
The Journal of Pediatrics|May 1, 1974
Plasma and erythrocyte folate levels in low-birth-weight infantsE D Hibbard, D Obst, A P Kenna
Lancet (London, England)|May 16, 1981
Life-threatening illness in those with severe mental handicapA N Campbel, J R Beasley, A P Kenna
Developmental Medicine and Child Neurology|October 1, 1991
Familial infantile myasthenia: a diagnostic problemJ W Matthes, A P Kenna, P R Fawcett
Clinical Genetics|July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the diseaseP Humphries, G J Farrar, P Kenna, et al.
The Quarterly Journal of Medicine|January 1, 1975
Congenital heart disease in Liverpool: 1960--69A P Kenna, R W Smithells, D W Fielding
Human Mutation|January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, et al.
Human Mutation|March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variantsKevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 1, 1995
No evidence of Chlamydia trachomatis infection in children with wheezeP L Ragunathan, J W Gray, A P Kenna, et al.
Experimental Eye Research|April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouseM Campbell, M Humphries, A Kennan, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Science (New York, N.Y.)|May 8, 1992
On the molecular genetics of retinitis pigmentosaP Humphries, P Kenna, G J Farrar
The Journal of Pediatrics|May 1, 1974
Plasma and erythrocyte folate levels in low-birth-weight infantsE D Hibbard, D Obst, A P Kenna
Lancet (London, England)|May 16, 1981
Life-threatening illness in those with severe mental handicapA N Campbel, J R Beasley, A P Kenna
Developmental Medicine and Child Neurology|October 1, 1991
Familial infantile myasthenia: a diagnostic problemJ W Matthes, A P Kenna, P R Fawcett
Clinical Genetics|July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the diseaseP Humphries, G J Farrar, P Kenna, et al.
The Quarterly Journal of Medicine|January 1, 1975
Congenital heart disease in Liverpool: 1960--69A P Kenna, R W Smithells, D W Fielding
Human Mutation|January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, et al.
Human Mutation|March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variantsKevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 1, 1995
No evidence of Chlamydia trachomatis infection in children with wheezeP L Ragunathan, J W Gray, A P Kenna, et al.
Experimental Eye Research|April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouseM Campbell, M Humphries, A Kennan, et al.
Pageof 8